Synthesis of (S)-N-ethyl-2-(5-methylene-4-oxocyclopent-2-en-1-yl)acetamide – a model exomethylidencyclopentenone bioisoster of prostamides
- Autores: Gimazetdinov A.M.1, Makaev Z.R.1, Miftakhov M.S.1
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Afiliações:
- UFRS RAS
- Edição: Volume 61, Nº 3 (2025)
- Páginas: 246-252
- Seção: ЭКСПЕРИМЕНТАЛЬНЫЕ СТАТЬИ
- URL: https://cardiosomatics.orscience.ru/0514-7492/article/view/687792
- DOI: https://doi.org/10.31857/S0514749225030049
- EDN: https://elibrary.ru/ETTOTN
- ID: 687792
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Resumo
The synthesis of the exo-methylidenecyclopentenone amide given in the title of the article from the methyl ester 2-{(1R,2R,5R)-2-[((tert-butyl(dimethyl)silyloxymethyl]-5-(trimethylsilyl)cyclopent-3-en-1-yl}acetic acid.
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Sobre autores
A. Gimazetdinov
UFRS RAS
Autor responsável pela correspondência
Email: gimazetdinov@anrb.ru
ORCID ID: 0000-0002-8539-3442
Ufa Institute of Chemistry
Rússia, prosp. Oktyabrya, 71, Ufa, 450054Z. Makaev
UFRS RAS
Email: gimazetdinov@anrb.ru
ORCID ID: 0000-0002-0958-3164
Ufa Institute of Chemistry
Rússia, prosp. Oktyabrya, 71, Ufa, 450054M. Miftakhov
UFRS RAS
Email: gimazetdinov@anrb.ru
Ufa Institute of Chemistry
Rússia, prosp. Oktyabrya, 71, Ufa, 450054Bibliografia
- Gimazetdinov A.M., Khalfitdinova L.A., Miftakhov M.S. Mendeleev Commun. 2013, 23, 321–322. doi: 10.1016/j.tet.2013.09.047
- Vostricov N.S., Spirikhin L.V., Lobov A.N., Gimazetdinov A.M., Zileeva Z.R., Vakhitova Y.V., Macaev Z.R., Pivnitsky K.K., Miftakhov M.S. Mendeleev Commun. 2019, 29, 372–374. doi: 10.1016/j.mencom.2019.07.003
- Лоза В.В., Гимазетдинов А.М., Мифтахов М.С. ЖОрХ. 2018, 54, 1575–1620. [Loza V.V., Gimazetdinov A.M., Miftakhov M.S. Russ. J. Org. Chem. 2018, 54, 1585–1629.] doi: 10.1134/S1070428018110015
- Bie Q., Dong H., Jin C., Zhang H., Zhang B. Am. J. Transl. Res. 2018, 10, 648–658
- Ladin D.A., Soliman E., Escobedo R., Fitzgerald T.L., Yang L.V., Burns C., Dross R.V. Mol. Cancer Ther. 2017, 16, 838–849. doi: 10.1158/1535-7163.MCT-16-0484
- Ladin D.A., Nelson M.M., Cota E., Colonna C., Burns C., Robidoux J., Fisher-Wellman K.H., Van Dross-Anderson R. Oncotarget. 2022, 13, 1380–1396. doi: 10.18632/oncotarget.28334
- Gimazetdinov A.M., Gataullin S.S., Bushmarinov I.S., Miftakhov M.S. Tetrahedron. 2012, 68, 5754–5758. doi: 10.1016/j.tet.2012.05.036
- Гимазетдинов А.М., Альмухаметов А.З., Мифтахов М.С. ЖОрХ. 2019, 55, 938–944. [Gimazetdinov A.M., Al’mukhametov A.Z., Miftakhov M.S. Russ. J. Org. Chem. 2019, 55, 831–836.] doi: 10.1134/S1070428019060137
- Аралбаева Г.В., Альмухаметов А.З., Гимазетдинов А.М. ЖОрХ. 2022, 58, 1168–1180. [Aralbaeva G.V., Al’mukhametov A.Z., Gimazetdinov A.M. Russ. J. Org. Chem. 2022, 58, 1589–1599.] doi: 10.1134/S1070428022110057
- Gimazetdinov A.M., Al’mukhametov A.Z., Loza V.V., Spirikhin L.V., Miftakhov M.S. Mendeleev Commun. 2018, 28, 546–547. doi: 10.1016/j.mencom.2018.09.033
- Gimazetdinov A.M., Al’mukhametov A.Z., Miftakhov M.S. New J. Chem. 2022, 46, 6708–6714. doi: 10.1039/d2nj01003h
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